Headstart, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Headstart, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Elk Grove Village, US.
Last cleared in 2021. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Headstart, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
1 devices